Mrps9 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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42 records found for search term Mrps9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329367856	CV2457139	single nucleotide variant	NM_182640.3(MRPS9):c.25G>A (p.Gly9Ser)	not specified [RCV004264914]	uncertain significance	2	105038117	105038117	Human		name
597634723	CV3557476	single nucleotide variant	NM_182640.3(MRPS9):c.16G>A (p.Val6Met)	not specified [RCV004831026]	uncertain significance	2	105038108	105038108	Human		name
597634734	CV3557478	single nucleotide variant	NM_182640.3(MRPS9):c.17T>A (p.Val6Glu)	not specified [RCV004831028]	uncertain significance	2	105038109	105038109	Human		name
156243588	CV2231524	single nucleotide variant	NM_182640.3(MRPS9):c.32C>T (p.Ala11Val)	not specified [RCV004096586]	uncertain significance	2	105038124	105038124	Human		name
401924726	CV2812191	single nucleotide variant	NM_182640.3(MRPS9):c.711G>A (p.Glu237=)	not provided [RCV003436088]	likely benign	2	105092460	105092460	Human		name
597634729	CV3557477	single nucleotide variant	NM_182640.3(MRPS9):c.82C>G (p.Gln28Glu)	not specified [RCV004831027]	uncertain significance	2	105038174	105038174	Human		name
598179379	CV3993588	single nucleotide variant	NM_182640.3(MRPS9):c.693G>T (p.Ser231=)	not specified [RCV005371920]	likely benign	2	105092442	105092442	Human		name
156181011	CV2201784	single nucleotide variant	NM_182640.3(MRPS9):c.245A>G (p.Asn82Ser)	not specified [RCV004082224]	uncertain significance	2	105049280	105049280	Human		name
329399477	CV2470115	single nucleotide variant	NM_182640.3(MRPS9):c.269A>G (p.Asn90Ser)	not specified [RCV004287370]	uncertain significance	2	105049304	105049304	Human		name
401745239	CV2698497	single nucleotide variant	NM_182640.3(MRPS9):c.248T>C (p.Ile83Thr)	not specified [RCV004298997]	uncertain significance	2	105049283	105049283	Human		name
405743512	CV3368058	single nucleotide variant	NM_182640.3(MRPS9):c.116A>C (p.Gln39Pro)	not specified [RCV004498125]	uncertain significance	2	105038208	105038208	Human		name
405743526	CV3368060	single nucleotide variant	NM_182640.3(MRPS9):c.201A>C (p.Glu67Asp)	not specified [RCV004498127]	uncertain significance	2	105049236	105049236	Human		name
156360480	CV2269046	single nucleotide variant	NM_182640.3(MRPS9):c.721G>T (p.Val241Leu)	not specified [RCV004130230]	uncertain significance	2	105092470	105092470	Human		name
156186772	CV2324753	single nucleotide variant	NM_182640.3(MRPS9):c.758A>T (p.Lys253Ile)	not specified [RCV004172989]	uncertain significance	2	105092507	105092507	Human		name
156156865	CV2359890	single nucleotide variant	NM_182640.3(MRPS9):c.729G>C (p.Arg243Ser)	not specified [RCV004212741]	uncertain significance	2	105092478	105092478	Human		name
155988484	CV2363987	single nucleotide variant	NM_182640.3(MRPS9):c.982G>A (p.Val328Met)	not specified [RCV004218953]	uncertain significance	2	105097207	105097207	Human		name
156054786	CV2393104	single nucleotide variant	NM_182640.3(MRPS9):c.445T>G (p.Tyr149Asp)	not specified [RCV004226586]	uncertain significance	2	105080018	105080018	Human		name
329380974	CV2440458	single nucleotide variant	NM_182640.3(MRPS9):c.895G>A (p.Asp299Asn)	not specified [RCV004256390]	uncertain significance	2	105093604	105093604	Human		name
401723200	CV2724813	single nucleotide variant	NM_182640.3(MRPS9):c.629T>G (p.Val210Gly)	not specified [RCV004317810]	uncertain significance	2	105089973	105089973	Human		name
401863036	CV2755808	single nucleotide variant	NM_182640.3(MRPS9):c.446A>G (p.Tyr149Cys)	not specified [RCV004342180]	uncertain significance	2	105080019	105080019	Human		name
401899776	CV2762237	single nucleotide variant	NM_182640.3(MRPS9):c.382C>G (p.Pro128Ala)	not specified [RCV004335362]	uncertain significance	2	105071462	105071462	Human		name
401916751	CV2812190	single nucleotide variant	NM_182640.3(MRPS9):c.553C>T (p.Leu185Phe)	not provided [RCV003429216]	uncertain significance	2	105089047	105089047	Human		name
401924728	CV2812192	single nucleotide variant	NM_182640.3(MRPS9):c.734G>A (p.Arg245Gln)	not provided [RCV003436089]	likely benign	2	105092483	105092483	Human		name
405743698	CV3368086	single nucleotide variant	NM_182640.3(MRPS9):c.491A>C (p.Asp164Ala)	not specified [RCV004498153]	uncertain significance	2	105088985	105088985	Human		name
405743736	CV3368091	single nucleotide variant	NM_182640.3(MRPS9):c.580G>A (p.Val194Met)	not specified [RCV004498158]	uncertain significance	2	105089924	105089924	Human		name
405743834	CV3368105	single nucleotide variant	NM_182640.3(MRPS9):c.842C>T (p.Ala281Val)	not specified [RCV004498172]	uncertain significance	2	105093551	105093551	Human		name
407474885	CV3450468	single nucleotide variant	NM_182640.3(MRPS9):c.826A>G (p.Arg276Gly)	not specified [RCV004638273]	uncertain significance	2	105093535	105093535	Human		name
407474899	CV3450471	single nucleotide variant	NM_182640.3(MRPS9):c.920C>G (p.Thr307Arg)	not specified [RCV004638276]	uncertain significance	2	105093629	105093629	Human		name
407525229	CV3450472	single nucleotide variant	NM_182640.3(MRPS9):c.863A>G (p.His288Arg)	not specified [RCV004631680]	uncertain significance	2	105093572	105093572	Human		name
597634718	CV3557475	single nucleotide variant	NM_182640.3(MRPS9):c.998C>T (p.Ser333Leu)	not specified [RCV004831025]	uncertain significance	2	105097223	105097223	Human		name
597634739	CV3557479	single nucleotide variant	NM_182640.3(MRPS9):c.572C>G (p.Thr191Ser)	not specified [RCV004831029]	uncertain significance	2	105089066	105089066	Human		name
597634745	CV3557480	single nucleotide variant	NM_182640.3(MRPS9):c.434G>C (p.Arg145Pro)	not specified [RCV004831030]	uncertain significance	2	105080007	105080007	Human		name
597634750	CV3557481	single nucleotide variant	NM_182640.3(MRPS9):c.455A>G (p.Tyr152Cys)	not specified [RCV004831031]	uncertain significance	2	105080028	105080028	Human		name
598213546	CV3993585	single nucleotide variant	NM_182640.3(MRPS9):c.926A>G (p.Asp309Gly)	not specified [RCV005378367]	uncertain significance	2	105093635	105093635	Human		name
598213552	CV3993586	single nucleotide variant	NM_182640.3(MRPS9):c.701G>A (p.Gly234Asp)	not specified [RCV005378368]	uncertain significance	2	105092450	105092450	Human		name
598213556	CV3993587	single nucleotide variant	NM_182640.3(MRPS9):c.706G>T (p.Ala236Ser)	not specified [RCV005378369]	uncertain significance	2	105092455	105092455	Human		name
155996617	CV2393207	single nucleotide variant	NM_182640.3(MRPS9):c.1078G>A (p.Glu360Lys)	not specified [RCV004226678]	uncertain significance	2	105097303	105097303	Human		name
401748178	CV2698949	single nucleotide variant	NM_182640.3(MRPS9):c.1175C>T (p.Thr392Met)	not specified [RCV004303485]	uncertain significance	2	105099745	105099745	Human		name
405743451	CV3368050	single nucleotide variant	NM_182640.3(MRPS9):c.1088G>T (p.Trp363Leu)	not specified [RCV004498117]	uncertain significance	2	105097313	105097313	Human		name
405743487	CV3368055	single nucleotide variant	NM_182640.3(MRPS9):c.1123C>T (p.Arg375Cys)	not specified [RCV004498122]	uncertain significance	2	105099693	105099693	Human		name
407474890	CV3450469	single nucleotide variant	NM_182640.3(MRPS9):c.1084G>A (p.Glu362Lys)	not specified [RCV004638274]	uncertain significance	2	105097309	105097309	Human		name
407474893	CV3450470	single nucleotide variant	NM_182640.3(MRPS9):c.1072G>A (p.Glu358Lys)	not specified [RCV004638275]	uncertain significance	2	105097297	105097297	Human		name

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